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Human Heredity
|
January 1, 1987
Placental soluble aconitase: population studies in Italy
R Scacchi, R M Corbo, E Calzolari, et al.
American Journal of Medical Genetics
|
April 1, 1994
Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies
A Sensi, V Bettoli, M R Zampino, et al.
Patologia E Clinica Ostetrica E Ginecologica
|
March 1, 1982
[Aspect of the cytological endometrial smear obtained from a removed IUD and its relationship to the clinical tolerance of the device]
E Calzolari, D Eleuteri-serpieri, R Morelli, et al.
Human Genetics
|
November 1, 1992
Characterization and mapping of the 5' portion of von Willebrand factor pseudogene
P Patracchini, G Marchetti, V Aiello, et al.
Prenatal Diagnosis
|
June 22, 2000
Prenatal UPD testing survey in Robertsonian translocations
F Gualandi, A Sensi, C Trabanelli, et al.
Journal of Medical Genetics
|
August 1, 1986
Aetiological factors in hypospadias
E Calzolari, M R Contiero, E Roncarati, et al.
Minerva Ginecologica
|
May 1, 1988
[Experience with intrauterine contraception. Survey of 600 IUD users at the S. Anna University Hospital in Rome]
E Calzolari, C Girolametti, C Parisi, et al.
Clinical Genetics
|
June 1, 1996
Branchio-oto (BO) syndrome and oculo-auriculo-vertebral phenotype: overlapping clinical findings in a child from a BO family
A Sensi, G Cocchi, A Martini, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita
|
June 21, 2001
[Teratogenic effects of environmental lead exposure: a population case-control study]
M Vinceti, S Rovesti, E Calzolari, et al.
Patologia E Clinica Ostetrica E Ginecologica
|
January 1, 1987
[Oral contraceptives and their minor side effects: comparison of three low-dose estroprogestinic combinations]
G Perrone, E Calzolari, M Mancone, et al.
Page
of 14
Search research articles
Search
Showing results (51-60 of 135) with videos related to
Sort By:
Page
of 14
Human Heredity
|
January 1, 1987
Placental soluble aconitase: population studies in Italy
R Scacchi, R M Corbo, E Calzolari, et al.
American Journal of Medical Genetics
|
April 1, 1994
Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies
A Sensi, V Bettoli, M R Zampino, et al.
Patologia E Clinica Ostetrica E Ginecologica
|
March 1, 1982
[Aspect of the cytological endometrial smear obtained from a removed IUD and its relationship to the clinical tolerance of the device]
E Calzolari, D Eleuteri-serpieri, R Morelli, et al.
Human Genetics
|
November 1, 1992
Characterization and mapping of the 5' portion of von Willebrand factor pseudogene
P Patracchini, G Marchetti, V Aiello, et al.
Prenatal Diagnosis
|
June 22, 2000
Prenatal UPD testing survey in Robertsonian translocations
F Gualandi, A Sensi, C Trabanelli, et al.
Journal of Medical Genetics
|
August 1, 1986
Aetiological factors in hypospadias
E Calzolari, M R Contiero, E Roncarati, et al.
Minerva Ginecologica
|
May 1, 1988
[Experience with intrauterine contraception. Survey of 600 IUD users at the S. Anna University Hospital in Rome]
E Calzolari, C Girolametti, C Parisi, et al.
Clinical Genetics
|
June 1, 1996
Branchio-oto (BO) syndrome and oculo-auriculo-vertebral phenotype: overlapping clinical findings in a child from a BO family
A Sensi, G Cocchi, A Martini, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita
|
June 21, 2001
[Teratogenic effects of environmental lead exposure: a population case-control study]
M Vinceti, S Rovesti, E Calzolari, et al.
Patologia E Clinica Ostetrica E Ginecologica
|
January 1, 1987
[Oral contraceptives and their minor side effects: comparison of three low-dose estroprogestinic combinations]
G Perrone, E Calzolari, M Mancone, et al.
Page
of 14